Technology

TP-317: A Stable, Oral RvE1 Drug Designed for Clinical Development

TP-317 Stability Breakthrough

RVE1 CHALLENGE

RvE1, a potent lipid mediator, is extremely vulnerable to oxidative degradation ― impeding clinical development.

TP-317 SOLUTION

A novel small molecule of RvE1 that maintains stability as an oral formulation where previous attempts failed.

PATH FORWARD

TP-317 enables scalable manufacturing, extended shelf-life, predictable drug delivery, and IP protection to 2048.

Oral TP-317 Performance in Phase 1a Guides Dose Selection for Phase 1b

Oral Formulation

Releases RvE1 in the upper intestine
for systemic absorption

Safety & PK

Well tolerated with
dose-proportional pharmacokinetics

Target Coverage

RvE1 blood levels sufficient to
activate BLT1 at all doses

Layered IP Protection

TP-317 is protected by composition of matter patents in the U.S. and internationally.

Multiple Patent Families

Family #1: Granted: US, EU, Asia

Family #2: Granted: US │ Pending: ROW

Manufacturing Trade Secrets

Strong barriers to generic entry